Abstract

New strategies for profound inhibition of platelet activity at the injured coronary plaque focus on blockade of the platelet surface membrane glycoprotein IIb/IIIa receptor, which binds circulating fibrinogen or von Willebrand factor and crosslinks platelets as the final common pathway to platelet aggregation. Intravenous agents directed against this receptor include the chimeric monoclonal antibody fragment abciximab, the peptide inhibitor eptifibatide and nonpeptide mimetics tirofiban and lamifiban. Over 33,000 patients have been evaluated in 11 large-scale, placebo-controlled trials of these agents. During percutaneous coronary intervention, an absolute reduction of 1.5% to 6.5% in the 30-day risk of death, myocardial infarction or repeat urgent revascularization has been observed, with some variability in treatment effect among the agents tested (abciximab, eptifibatide and tirofiban). Treatment effect is achieved early with every modality of revascularization and is maintained over the long-term (up to three years). Increased bleeding risk may be minimized by reduction and weight-adjustment of concomitant heparin dosing. In the acute coronary syndromes without ST segment elevation, absolute 1.5% to 3.2% reductions in 30-day rates of death or myocardial (re-) infarction have been achieved with two to four day courses of eptifibatide or tirofiban. Clinical benefit accrues during the period of drug infusion and is durable. Treatment effect may be enhanced among patients undergoing early coronary revascularization, with evidence of stabilization before intervention and suppression of postprocedural ischemic events. Thus, blockade of the platelet glycoprotein IIb/IIIa receptor reduces ischemic complications when used as an adjunct to percutaneous coronary intervention or the management of acute ischemic syndromes.

Keywords

EptifibatideTirofibanMedicineAbciximabPercutaneous coronary interventionCardiologyInternal medicineMyocardial infarctionRevascularizationCoronary artery diseaseBlockadeAnesthesiaPharmacologyReceptor

MeSH Terms

AbciximabAcetatesAngioplastyBalloonCoronaryAntibodiesMonoclonalAnticoagulantsCombined Modality TherapyCoronary DiseaseDrug MonitoringEptifibatideHemorrhageHumansImmunoglobulin Fab FragmentsInfusionsIntravenousMyocardial InfarctionPatient SelectionPeptidesPlatelet Aggregation InhibitorsPlatelet Glycoprotein GPIIb-IIIa ComplexPractice Guidelines as TopicRecurrenceRisk FactorsTirofibanTreatment OutcomeTyrosine

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Publication Info

Year
2000
Type
review
Volume
35
Issue
5
Pages
1103-1115
Citations
197
Access
Closed

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197
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Cite This

A. Michael Lincoff, Robert M. Califf, Eric J. Topol (2000). Platelet glycoprotein IIb/IIIa receptor blockade in coronary artery disease. Journal of the American College of Cardiology , 35 (5) , 1103-1115. https://doi.org/10.1016/s0735-1097(00)00554-4

Identifiers

DOI
10.1016/s0735-1097(00)00554-4
PMID
10758948

Data Quality

Data completeness: 86%